Phase I/II, Multicenter, Open-label, Clinical and Pharmacokinetic Study of Lurbinectedin in Combination With Irinotecan in Pretreated Patients With Selected Advanced Solid Tumors

Study Identifier:
PM1183-A-014-15
CT.gov Identifier:
NCT02611024
EudraCT Identifier:
2015-003602-16
EU Trial (CTIS) Number:
2024-515394-10-00
Study Contact Information:
(210) 593-5651 or [email protected]
Study Complete

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Study Summary

To determine the maximum tolerated dose (MTD) and the recommended dose (RD) of PM01183 in combination with irinotecan in patients with selected advanced solid tumors

To analyze the safety profile, along with the handling of lurbinectedin and irinotecan in the study population

To obtain preliminary information on the antitumoral activity of PM01183 in combination with irinotecan

To evaluate the pharmacogenomics with tumor samples from patients exposed to both compounds in order to assess potential markers to both response and/or resistance

To evaluate escalating doses of LUR on Day (D) 1 plus a fixed dose of IRI 75mg/m2 on D1 and D8 every 3 weeks (q3w) in pts with advanced solid tumors, enrolled following a standard 3+3 dose escalation design

To evaluate escalating doses of LUR on Day (D) 1 plus a fixed dose of IRI 75 mg/m2 on D1 and D8 every 3 weeks (q3w) in pts with advanced solid tumors (+/- G-CSF, if dose-limiting toxicities [DLTs] were neutropenia)

Phase I: escalating doses of LUR on day 1 plus a fixed dose of IRI 75 mg/m2 on day 1 and day 8 every 3 weeks (q3w) in patients (pts) with advanced solid tumors, following a standard 3+3 dose-escalation design

  • Phase Il expansion at the recommended dose (RD) to further explore efficacy and safety in indications where antitumor activity or a signal of activity was observed during phase I dose escalation
Medical Condition
The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.
Solid Tumor
Brain
Unmapped
Endometrial
Ovarian
Mesothelioma
Unmapped
Small Cell Lung
Unmapped
Pancreas
Bowel (Colorectal)
Neuroendocrine
Phase
The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
Phase I/II
Sex
Female & Male
Age
18 - 70 Years
Study Drug
Drug: Experimental: Lurbinectedin Escalation Group
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Drug: Experimental: Irinotecan Escalation Group
Drug: Experimental: Intermediate Escalation Group
Drug: Drug: Lurbinectedin
Drug: Drug: Irinotecan
Drug: ASCO 2021:
Drug: lurbinectedin- 4mg, Intravenous
Drug: Two groups evaluated a schedule of lurbinectedin on Day (D)1 every three weeks (q3wk) combined with irinotecan on D1,D8 q3wk: the lurbinectedin escalating group (escalating doses of lurbinectedin plus fixed irinotecan dose of 75 mg/m2) and the irinotecan D1,D8 escalating group (fixed lurbinectedin dose of 3.0 mg/m2 plus escalating doses of irinotecan). The third group was the irinotecan D1 escalating group, which evaluated a schedule of a fixed lurbinectedin dose of 2.6 mg/m2 plus escalating doses of irinotecan, both on D1 q3wk. In all groups, lurbinectedin was administered as 1-h intravenous (i.v.) infusions and irinotecan as 90-min i.v. infusions. Treatment was administered until disease progression, unacceptable toxicity, intercurrent illness precluding study continuation, patient refusal and/or non-compliance with study requirements, treatment delay>15 days (except if with clear clinical benefit),>2 dose reductions per drug (irinotecan or lurbinectedin), and treatment-related grade≥3 rhabdomyolysis
Study Status
Indicates the current recruitment status or the expanded access status
Study Complete

Requirements information
Inclusion criteria
  • Voluntarily signed and dated written informed consent prior to any specific-study procedure.
  • Age ≥ 18 years.
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 1.
  • Life expectancy ≥ 3 months.
  • Histologically or cytologically confirmed diagnosis of advanced disease of any of the following tumor types:
  • For the Lurbinectedin Escalation Group and the Irinotecan Escalation Group:
  • Glioblastoma.
  • Soft-tissue sarcoma (excluding gastrointestinal stromal tumors [GIST]).
  • Endometrial carcinoma.
  • Epithelial ovarian carcinoma (including primary peritoneal disease and/or fallopian tube carcinomas and/or endometrial adenocarcinomas) regardless of platinum sensitivity.
  • Mesothelioma.
  • Gastroenteropancreatic neuroendocrine tumors (GEP-NET).
  • Small cell lung cancer (SCLC).
  • Pancreatic adenocarcinoma.
  • Gastric carcinoma.
  • Colorectal carcinoma (CRC).
  • For the Intermediate Escalation Group:
  • Endometrial carcinoma.
  • SCLC.
  • Other solid tumors may be included, if appropriate, after discussion between the Investigators and the Sponsor.
  • For the Phase II expansion stage:
  • Glioblastoma.
  • Soft tissue sarcoma (including synovial sarcoma),
  • Endometrial carcinoma.
  • SCLC.
  • Neuroendocrine tumors.
  • Group 1: Poorly differentiated grade 3 NEC (Ki-67 >20%) according to the 2019 WHO classification of tumors of the digestive system, of gastroenteropancreatic origin or unknown primary site (lung primary tumors will be excluded).
  • Group 2: Well differentiated grade 2 (Ki-67 3-20%) or grade 3 (Ki-67 21-55%) GEP-NETs according to the 2019 WHO classification of tumors of the digestive system.
  • The number of prior lines of therapy allowed per patient will be as follows:
  • For the Phase I Escalation Stage:
  • No more than two prior lines of cytotoxic-containing chemotherapy regimens for advanced disease
  • For the Phase II Lurbinectedin Expansion Stage:
  • For SCLC, one prior line of platinum-containing chemotherapy with/without antibodies against programmed cell death protein-1 (PD-1) or programmed death ligand-1 (PD-L1).
  • For NENs,
  • In Group 1 (patients with poorly differentiated NEC of gastroenteropancreatic origin or unknown primary site, excluding lung primary tumors), one prior line of platinum-based chemotherapy; and
  • In Group 2 (patients with well differentiated GEP-NETs), no more than three prior lines of systemic therapy (that may include somatostatin analogues, chemotherapy, everolimus and/or sunitinib).
  • For all other tumor types, no more than two prior lines of cytotoxic-containing chemotherapy regimens for advanced disease.
  • There is no limit for prior targeted therapy, hormonal therapy and immunotherapy (such as nivolumab).
  • Phase II expansion stage: Tumor-specific cohort(s) at the RD:
  • Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) v.1.1. For patients with glioblastoma: Measurable disease according to RECIST v.1.1 and Response Assessment in Neuro-Oncology (RANO) criteria.
  • Documented disease progression per RECIST v.1.1 during or immediately after last therapy according to any of the aforementioned criteria. For patients with glioblastoma: Documented disease progression per RECIST v.1.1 and RANO criteria.
  • At least three weeks since the last anticancer therapy, (including immunotherapy, investigational drugs and radiotherapy), and at least six weeks since nitrosoureas and mitomycin C (systemic).
  • For biological/investigational anticancer therapies given orally, the aforementioned period of at least three weeks could be changed for one of at least five half-lives (whichever occurred first), provided that the therapy is given as single agent and not combined with other drugs. If this is not the case, this exception will not be acceptable.
  • For patients with glioblastoma: at least 12 weeks since the end of radiotherapy, except if:
  • The patient has a new lesion outside of the radiotherapy field, or
  • The patient has undergone brain surgery to remove the tumor before study entry, and progressive disease has been confirmed histologically.
  • Note: washout periods will be referred to the day of first cycle administration (Day 1), not to the day of registration (Day 0).
  • Adequate bone marrow, renal, hepatic, and metabolic function (assessed ≤ 7 days before inclusion in the trial):
  • Platelet count ≥ 100 × 10^9/L, hemoglobin ≥ 9.0 g/dL and absolute neutrophil count (ANC) ≥ 2.0 × 10^9/L.
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3.0 × the upper limit of normal (ULN), even in the presence of liver metastases.
  • Alkaline phosphatase (ALP) ≤ 2.5 × ULN (≤ 5 × ULN if disease-related/in the case of liver metastases).
  • Total bilirubin ≤ 1.5 × ULN or direct bilirubin ≤ ULN.
  • International Normalized Ratio (INR) < 1.5 (except if patient is on oral anticoagulation therapy).
  • Calculated creatinine clearance (CrCL) ≥ 30 mL/minute (using Cockcroft-Gault formula).
  • Creatine phosphokinase (CPK) ≤ 2.5 × ULN.
  • Albumin ≥ 3.0 g/dL*
  • Recovery to grade ≤ 1 or to baseline from any adverse event (AE) derived from previous treatment (excluding alopecia and/or cutaneous toxicity and/or peripheral neuropathy and/or fatigue grade ≤ 2).
  • Albumin transfusion to increase the blood level in order to fulfill the inclusion criterion is strictly forbidden.
  • This cohort included pts with SS progressing after up to 2 prior cytotoxic-containing lines for advanced disease
Exclusion criteria
  • Concomitant diseases/conditions:
  • History or presence of unstable angina, myocardial infarction, congestive heart failure, or clinically significant valvular heart disease within the previous year.
  • Symptomatic arrhythmia or any uncontrolled arrhythmia requiring ongoing treatment.
  • Myopathy or any clinical situation that causes significant and persistent elevation of CPK (> 2.5 × ULN in two different determinations performed one week apart).
  • Ongoing chronic alcohol consumption or cirrhosis with Child-Pugh score B or C. Known Gilbert disease.
  • Active uncontrolled infection.
  • Known human immunodeficiency virus (HIV) or known hepatitis C virus (HCV) infection or active hepatitis B.
  • Any past or present chronic inflammatory colon and/or liver disease, past intestinal obstruction, pseudo or sub-occlusion or paralysis.
  • Evident symptomatic pulmonary fibrosis or interstitial pneumonitis, pleural or cardiac effusion rapidly increasing and/or necessitating prompt local treatment within seven days.
  • Any other major illness that, in the Investigator's judgment, will substantially increase the risk associated with the patient's participation in this study
  • Active Coronavirus disease (COVID-19).
  • Hypersensitivity to any of the study drugs or their excipients.
  • Prior treatment with lurbinectedin, trabectedin (Yondelis) or topoisomerase I inhibitors (irinotecan, topotecan, etc.). Prior topoisomerase inhibitors (e.g., irinotecan) are only allowed in patients with colorectal carcinoma or NENs.
  • Prior bone marrow or stem cell transplantation, or radiation therapy in more than 35% of bone marrow.
  • Known brain metastases or leptomeningeal disease involvement. Glioblastoma lesions (primary or locally advanced) are eligible. Exception: patients with brain metastases are eligible provided they are radiologically stable, i.e. without evidence of progression for at least 4 weeks by repeat imaging (note that the repeat imaging should be performed during study screening), clinically stable and without requirement of steroid treatment (patients taking steroids in the process of already being tapered within two weeks prior to screening are allowed). Brain CT-scan or MRI results must be provided at baseline.
  • Women who are pregnant or breast feeding and fertile patients (men and women) who are not using an effective method of contraception. Women of childbearing potential (WOCBP) must agree to use an effective contraception method to avoid pregnancy during the course of the trial (and for at least six months after the last infusion). Fertile male patients must agree to refrain from fathering a child or donating sperm during the trial and for four months after the last infusion.
  • Limitation of the patient's ability to comply with the treatment or follow-up protocol.

Clinical Study Information for Healthcare Providers

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Study Locations

Location
Investigator
Status
Condition(s) Treated at Site
Location
START Madrid, Spain (CIOCC)
Madrid, Spain, 28050
Investigator
Maria de Miguel
Status
Terminated/Withdrawn
Condition(s) Treated at Site
Solid Tumor
Brain
Unmapped
Endometrial
Ovarian
Mesothelioma
Unmapped
Small Cell Lung
Unmapped
Pancreas
Bowel (Colorectal)
Neuroendocrine